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二氮嗪或多粘菌素B对分离的大鼠红细胞或脂肪细胞葡萄糖转运的抑制作用。

Inhibitory effects of diazoxide or polymyxin B on glucose transport by isolated rat erythrocytes or adipocytes.

作者信息

Goto Y, Kida K, Kaino Y, Ito T, Matsuda H

机构信息

Department of Pediatrics, Ehime University School of Medicine, Japan.

出版信息

Acta Paediatr Jpn. 1994 Dec;36(6):637-41. doi: 10.1111/j.1442-200x.1994.tb03260.x.

Abstract

The inhibitory effects of diazoxide or polymyxin B on 3-O-methylglucose uptake were studied in isolated rat erythrocytes or adipocytes to elucidate the mechanisms of the actions of these agents. One to three mmol/L diazoxide significantly inhibited 3-O-methylglucose uptake into erythrocytes by 11-33% without altering the equilibrium space, while 0.3 mmol/L diazoxide did not. The inhibitory effect was exerted in a dose-dependent manner in this concentration range. To test whether polymyxin B affects the process of insulin action or the glucose transport activity recruited by insulin, adipocytes prestimulated with insulin and exposed to 2 mmol/L potassium cyanide (KCN) were employed since the cells, on which glucose transporters recruited by insulin were located quiescently, were useful to estimate the effect of an agent on glucose transport activity per se. Polymyxin B (100 micrograms/mL) inhibited the insulin-stimulated uptake activity in this transport system by 22.5% while it inhibited the insulin-stimulated uptake activity in intact adipocytes which were not exposed to KCN by 32.2%. These results suggest that diazoxide inhibits the function of the erythrocyte glucose transporter, GLUT1 (classified by Bell et al.), and indicate that the inhibition of the glucose transport activity recruited by insulin is the major effect of polymyxin B (100 micrograms/mL) and the inhibition of the process of insulin action is rather small.

摘要

研究了二氮嗪或多粘菌素B对分离的大鼠红细胞或脂肪细胞中3 - O - 甲基葡萄糖摄取的抑制作用,以阐明这些药物的作用机制。1至3 mmol/L的二氮嗪显著抑制红细胞对3 - O - 甲基葡萄糖的摄取,抑制率为11% - 33%,且不改变平衡空间,而0.3 mmol/L的二氮嗪则无此作用。在该浓度范围内,抑制作用呈剂量依赖性。为了测试多粘菌素B是否影响胰岛素作用过程或胰岛素募集的葡萄糖转运活性,使用预先用胰岛素刺激并暴露于2 mmol/L氰化钾(KCN)的脂肪细胞,因为胰岛素募集的葡萄糖转运蛋白静止存在的这些细胞,有助于评估药物对葡萄糖转运活性本身的影响。多粘菌素B(100微克/毫升)在该转运系统中抑制胰岛素刺激的摄取活性22.5%,而在未暴露于KCN的完整脂肪细胞中抑制胰岛素刺激的摄取活性32.2%。这些结果表明,二氮嗪抑制红细胞葡萄糖转运蛋白GLUT1(由贝尔等人分类)的功能,并表明多粘菌素B(100微克/毫升)对胰岛素募集的葡萄糖转运活性的抑制是主要作用,而对胰岛素作用过程的抑制作用较小。

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